简介:Whitelight-emittingYVO_4:1mol.%Dy~(3+),xmol.%Eu~(3+)phosphorpowderswithordermorphologyandwellcrystallizationwerehydrothermallysynthesizedat180°C.Themicrostructure,white-lightemission,andlight-emittingmechanismofthepowderswerecarefullystudiedusingX-raydiffractometry,scanningelectronmicroscopyandphotoluminescencespectra.TheexcitationandemissionspectraofthephosphorpowdersindicatedthecoexistenceofefficientenergytransferfromEu~(3+)toDy~(3+)andinefficientenergytransferfromDy~(3+)toEu~(3+)besidestheenergytransferfromVO_4~(3–)toEu~(3+).IncreasingtheEu~(~(3+))concentrationinitiallyenhancedandthenweakenedtheluminescentintensityofDy~(3+).Thewhite-lightemissionsofYVO_4:1mol.%Dy~(3+),xmol.%Eu~(3+)phosphorpowderswerebothrelatedtotheenergytransferbetweenVO_4~(3–)andDy~(3+)/Eu~(3+),aswellasbetweenEu~(3+)andDy~(3+).TheinefficientenergytransferfromDy~(3+)toEu~(3+)wasfirstfound.
简介:Eu-activatedCaMoO4phosphorswereco-precipitatedinanaqueoussolution,andNH3·H2O,NH4HCO3and(NH2)2COaspre-cipitatingaidagentswerecomparedbasedonthemorphologyandparticlesizedistributionofthephosphorsamples.Sm3+assensitizerionwasinvestigatedontheluminescenceofCaMoO4:Eu,anditcouldstrengthenthe406nmabsorptionofthisphosphor.Atlast,thescheeliteCaMoO4:EuandwolframiteZnMoO4:Euwereselectedtocomparetheirhostabsorption.TheresultshowedthatthescheelitemolybdatehostexhibitedstrongerUVabsorptionthanwolframiteone.
简介:AseriesofMn-basedcatalysts,MnOx,MnOx-CeO2,Pd-Mn-Ce,MnOx/ACwereprepared.AndtheirperformancesforNOlow-temperatureSCRwereinvestigatedinthisstudy.TheNOconversionisabout90%at100℃onMnOx-CeO2andalmostallNOcanbeconvertedat120℃.SimilarresultsarealsoobservedinthetestsonMnOx-CeO2/AC.Theexcellentlow-temperaturecatalyticactivityofmodifiedMn-basedcatalysts,whichmaybemainlyduetotheoxygenstoragefunctionofCeO2,canimprovetheoxygenflowonthecatalystssurface.ThentheoxidationofNOtoNO2isaccelerated,whichisthekeystepofNOSCR.
简介:ThedopedZnOnanorodsasaphotocatalystwithdifferentEucontentswerepreparedbymicrowaveassistedmethodandtheywerecharacterizedbymeansofX-raydiffraction(XRD),energy-dispersiveX-rayspectroscopy(EDS),UV-Visspectroscopy,surfaceareaBrunauer-Emmett-Teller(BET),X-rayphotoelectronspectroscopy(XPS),scanningelectronmicroscopy(SEM)andtransmissionelectronmicroscopy(TEM).TheaveragecrystallitesizeandbandgapenergyofEu-dopedZnOwerevariedwiththeEucontent.TheXRDpatternofEu-dopedZnOindicatedhexagonalcrystalstructurewithanaveragecrystallitesizeof25nm.ThepresenceofeuropiumwithtrivalentstateanditsdopingsuccessfullyintothecrystallatticeofZnOmatrixwereconfirmedbyXPStechnique.ThephotocatalyticactivityofEu-dopedZnOnanorodswasevaluatedformethylorangedegradation.Thephotocatalyticexperimentsshowed~91%degradationofmethylorangeover0.2mol.%EudopedZnOsamplewithin3hunderUVlight(365nm).
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简介:NanosizedBaCeo.95Yo.o5O3-δpowderswiththehomogeneouscompositionweresynthesizedbyanewcombustionprocessbasedonthePechinimethod.Apolymericprecursorsolwasformedbyuseofcitricacidandethyleneglycolasthechelatingagentsofmetalions.Theperovskite-typeBaCeo.95Yo.o5O3-δpowderswithuniformshapeandsmallerthan40nminsizedwereobtainedthroughthecombustionofthepolymericprecursorsolattheexistenceofnitricacidandammoniumhydroxide.Itwasfoundtheparticlesizecouldbecontrolledbymodulatingthequantitiesofnitricacidandammoniumhydroxide,thequantitiesoftheresidue,carbonateionswerealsoaffectedbythequantitiesofthecitricacidandethyleneglycol.
简介:YbF2.357,YbF3,Ba2YbF7,andBa2upconversionnanocrystalsdopedwithemitterEr3+ionweresynthesizedinthesamesolventsystemjustwithchangingthemolarratioofBa2+toYb3+intheprecursor,whichcorresponedtothecrystalphasesofrhombohedral,orthorhombic,tetragonal,andcubic,respectively.Allthesamplesemittedboth660nmredlightand543/523nmgreenlightwhichoriginatedfromEr3+-4fnelectronictransitions4F9/2-4I15/2and4S3/2/2H11/2-4I15/2,respectively.ItwasworthmentioningthatYbF3:Er3+,Ba2YbF7:Er3+,andBaF2:Er3+couldemitdazzlinglybrightlightevenundertheexcitationofa980nmCWlaserwithoutputpowerof0.1W.Upconversionemissionmechanismanalysisindicatedthattheintensityratioofredtogreenlighthighlydependedonthesynergisticeffectofcrystalstructure,concentrationquenching,andparticlesize,butwerenotsensitivetocrystallinityaspreviouslyreportedforNaLnF4(Ln=lanthanide).
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简介:SmOHCO3micro/nanoparticleswerepreparedinwater/oil(W/O)reversemicroemulsioncomposedofcetyltrimethylammoniumbromide(CTAB),n-octane,n-butanol,Sm(NO3)3·6H2Oandureaaqueoussolutionbythecouplingrouteofhomogeneousprecipitationwithmicroemulsion.ThenanoparticleswerecharacterizedandanalyzedbyX-raypowderdiffraction(XRD),thermalgravimetricanddifferentialthermalgravimetricanalysis(TG-DTG),Fouriertransforminfraredabsorptionspectra(FT-IR)andscanningelectronmicroscope(SEM).TheresultsshowedthatthephaseSmOHCO3micro/nanoparticleswasinagreementwithpureorthorhombicphase.ThedifferentmorphologiesofSmOHCO3micro/nanoparticleswithgoodmonodispersityandsizewereobtainedbyregulatingthereactiontemperatureandreactiontime.PossibleformationmechanismsofthemorphologicalstructureofSmOHCO3wereproposedanddiscussed.
简介:黄磷(Bi1-xSmx)2ZnB2O7(x=0.01,0.03,0.05,0.07,和0.09)被常规稳固的州的反应综合。所有样品的纯净被X光检查粉末衍射(XRD)检查。XRD分析证明所有这些混合物具有Bi2ZnB2O7的一个单个阶段,显示在Bi2ZnB2O7的双性人(3+)能被没有晶体结构的变化的Sm(3+)部分代替。在房间温度的刺激和排放系列显示出Sm(3+)的典型4f-4f转变。主导的刺激线在404nm附近由于(6)H5/2→(4)K11/2和排放光谱在563,599,646,和704nm由一系列线组成由于(4)G5/2→(6)H5/2,(6)H7/2,(6)H9/2,并且(6)H11/2分别地。在Bi2ZnB2O7的Sm(3+)的最佳的集中关于3mol%(相对1mol双性人(3+))并且批评距离Rc作为2.1nm被计算。Bi1.94Sm0.06ZnB2O7的排放紧张的温度依赖在在100和450K之间的温度范围被检验。紧张下降了到起始的紧张的一半的熄灭的温度是280K。为在Bi1.94Sm0.06ZnB2O7的Sm(3+)的一生作为0.29和1.03ms的价值被适合。